US2762812A - Arylcycloalkenyl-tertiary-aminoalkyl acetonitriles - Google Patents
Arylcycloalkenyl-tertiary-aminoalkyl acetonitriles Download PDFInfo
- Publication number
- US2762812A US2762812A US306486A US30648652A US2762812A US 2762812 A US2762812 A US 2762812A US 306486 A US306486 A US 306486A US 30648652 A US30648652 A US 30648652A US 2762812 A US2762812 A US 2762812A
- Authority
- US
- United States
- Prior art keywords
- hydrochloride
- beta
- crude
- ether
- prepared
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000001875 compounds Chemical class 0.000 claims description 21
- 150000002825 nitriles Chemical class 0.000 claims description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 96
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 55
- -1 cycloalkenyl radicals Chemical class 0.000 description 51
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 49
- 238000000034 method Methods 0.000 description 36
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 31
- 239000000725 suspension Substances 0.000 description 28
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
- 239000000047 product Substances 0.000 description 24
- 150000003839 salts Chemical class 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 229950000188 halopropane Drugs 0.000 description 11
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 11
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 11
- 125000005853 β-dimethylaminoethyl group Chemical group 0.000 description 11
- 239000001294 propane Substances 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 9
- 238000001953 recrystallisation Methods 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 229940093499 ethyl acetate Drugs 0.000 description 8
- 235000019439 ethyl acetate Nutrition 0.000 description 8
- SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 description 7
- ZHOOOLQOWQVYOE-UHFFFAOYSA-N 2-cyclohexylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCCC1 ZHOOOLQOWQVYOE-UHFFFAOYSA-N 0.000 description 6
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 6
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 6
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 6
- 239000012259 ether extract Substances 0.000 description 6
- 239000012458 free base Substances 0.000 description 6
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- LQLJZSJKRYTKTP-UHFFFAOYSA-N 2-dimethylaminoethyl chloride hydrochloride Chemical compound Cl.CN(C)CCCl LQLJZSJKRYTKTP-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 239000013058 crude material Substances 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229960001340 histamine Drugs 0.000 description 3
- 150000007530 organic bases Chemical class 0.000 description 3
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WNRWEBKEQARBKV-UHFFFAOYSA-N 1-(2-chloroethyl)piperidine Chemical compound ClCCN1CCCCC1 WNRWEBKEQARBKV-UHFFFAOYSA-N 0.000 description 2
- VFLQQZCRHPIGJU-UHFFFAOYSA-N 1-(2-chloroethyl)piperidine;hydron;chloride Chemical compound Cl.ClCCN1CCCCC1 VFLQQZCRHPIGJU-UHFFFAOYSA-N 0.000 description 2
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- PACGLQCRGWFBJH-UHFFFAOYSA-N 2-(4-methoxyphenyl)acetonitrile Chemical compound COC1=CC=C(CC#N)C=C1 PACGLQCRGWFBJH-UHFFFAOYSA-N 0.000 description 2
- OMNFRAFCXNVDLP-UHFFFAOYSA-N 2-cyclopentylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCC1 OMNFRAFCXNVDLP-UHFFFAOYSA-N 0.000 description 2
- LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical compound NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 description 2
- 229930003347 Atropine Natural products 0.000 description 2
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 2
- 208000007101 Muscle Cramp Diseases 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 208000005392 Spasm Diseases 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 230000002921 anti-spasmodic effect Effects 0.000 description 2
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 2
- 229960000396 atropine Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
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- 150000004820 halides Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
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- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
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- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000001302 tertiary amino group Chemical group 0.000 description 2
- FSNGFFWICFYWQC-UHFFFAOYSA-N 1-(2-chloroethyl)pyrrolidine;hydron;chloride Chemical compound Cl.ClCCN1CCCC1 FSNGFFWICFYWQC-UHFFFAOYSA-N 0.000 description 1
- OBOBUDMMFXRNDO-UHFFFAOYSA-N 1-(3-chloropropyl)piperidine;hydron;chloride Chemical compound Cl.ClCCCN1CCCCC1 OBOBUDMMFXRNDO-UHFFFAOYSA-N 0.000 description 1
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 description 1
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- YMDNODNLFSHHCV-UHFFFAOYSA-N 2-chloro-n,n-diethylethanamine Chemical compound CCN(CC)CCCl YMDNODNLFSHHCV-UHFFFAOYSA-N 0.000 description 1
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- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
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- ZPDZEMBAZCBLGS-UHFFFAOYSA-N 3-cyclopentylidene-N,N-dimethyl-3-phenylpropan-1-amine Chemical compound CN(CCC(=C1CCCC1)C1=CC=CC=C1)C ZPDZEMBAZCBLGS-UHFFFAOYSA-N 0.000 description 1
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- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
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- 238000010521 absorption reaction Methods 0.000 description 1
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- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
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- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
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- 239000001273 butane Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
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- 239000000460 chlorine Substances 0.000 description 1
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- 229930192474 thiophene Natural products 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/145—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Definitions
- ti ycloalkylidene eyclyalkenyl These structures are isomeric, differing only in the position of the olefinic linkage: in Formula a the double bond is exocyclic, in Formula b endocyclic.
- the cycloalkylidene and cycloalkenyl radicals may contain five or six carbon atoms and R represents an aromatic group.
- aromatic embraces aryl groups such as phenyl, substituted phenyl, naphthyl, xenyl, etc. as Well as certain heterocyc'lic groups such as thienyl, pyridyl, furyl, etc.
- Formula I has the double bond in conjugation with the aromatic nucleus and tends to show a maximum of absorption at 240-250 mg with the logarithm of the molar extinction coeflicient (log EM) approximately 4, similar to that shown by styrene and substituted styrenes.
- log EM logarithm of the molar extinction coeflicient
- These compounds are generally used in the form of water-soluble salts such as those produced by the addition of acids.
- the acids which may be used to prepare the salts are those which produce, when combined with the free bases, salts whose anions are relatively innocuous to the animal organism in therapeutic doses of the salts, so that the beneficial physiological properties inherent in the free bases are not vitiated by side-efiects ascribable to the anions.
- Appropriate acid addition salts are those derived from mineral acids such as hydrochloric acid, hydrobromic acid, hydriodic acid and sulfuric acid; and organic acids such as acetic acid, citric acid and tartaric aid.
- Our compounds may also be used in the form of ammonium salts derived from lower alkyl esters of strong inorganic acids, organic sulfonic acids and the like, such as methyl chloride, methyl bromide, methyl iodide, ethyl bromide, ethyl iodide, propyl bromide, propyl iodide, methyl sulfate, methyl benzenesulfonate, methyl p-toluenesulfonate, etc.
- ammonium salts derived from lower alkyl esters of strong inorganic acids, organic sulfonic acids and the like, such as methyl chloride, methyl bromide, methyl iodide, ethyl bromide, ethyl iodide, propyl bromide, propyl iodide, methyl sulfate, methyl benzenesulfonate, methyl p-to
- Our compounds show consistently high antispasmodic and moderate antihistaminic activity. They are effective both against barium chloride induced spasms (musculotropic), showing'from ten to seventy times the activity of papaverine; and against acetylcholine induced spasms (neurotropic), showing from one to eight percent of the activity of atropine.
- atropine possesses a considerably higher neurotropic activity than our compounds and other synthetic antispasmodics, it produces many undesirable physiological side-efli'ects. It is therefore highly desirable to vfind synthetic drugs which do not induce these characteristic side reactions in the organism.
- Histamine has been demonstrated to play an important role in allergenic reactions, and it has been found that substances which are antagonistic to histamine often cause marked amelioration of symptoms.
- Our compounds have been found to be five to fifty times as efliective as papavcrime in counteracting the physiological eflFects of histamine.
- RCHzCN phenylacetonitrile, p-anisylacetonitrile, manisylacetonitrile, p-tolylacetonitrile, l-naphthalencacetonitrile, Z-naphthaleneacetonitrile, Z-thiopheneacetonitrile, 3-thiopheneacetonitrile, Z-furanacetonitrile, 3-furanacetonitrile, Z-pyridineacetonitrile and 4-pyridineacetonitrile.
- the expected structure is that of Formula III(a).
- a tautomeric shift of a hydrogen atom leads to the formation of the structure III(b) to a greater or less extent.
- X is a halogen
- X preferably chlorine, bromine or iodine
- X include beta-diethylaminoethyl halide, beta-dimethylaminoethyl halide, beta-(ethylmethylamino)-ethyl halide, beta-dipropylaminoethyl halide, beta-dibutylaminoethyl halide, 3-dimethylamino-l-halopropane, 3-diethylamino-l-halopropane, 1-dimethylamino-Z-halopropane, 1- diethylamino-Z-halopropane
- Example 1 (a) Cyclohexylidenephenylacetonitrile.-In a 2-liter, 3-necked flask, equipped with a stirrer, thermometer and dropping funnel, was placed 600 cc. of absolute ethyl alcohol, and 23 g. of sodium was dissolved therein. Benzyl cyanide (117 cc.) was then added, and, after cooling the mixture to room temperature, g. of cyclohexanone was added gradually through the dropping funnel with stirring. The reaction mixture was refluxed for 45 minutes, cooled, diluted with water and acidified with dilute hydrochloric acid.
- the hydrochloride was prepared by dissolving the free amine in dry ether and adding an excess of alcoholic hydrogen chloride- The crude solid which precipitated was filtered, recrystallized'once from isopropyl alcohol and twice from an absolute alcohol-dry ether mixture, giving 3.7 g. of the hydrochloride of l-(N-piperidyl)-3-phenyl-3-(A -cyclopentenyl)-propane, M. P. 227 C. (dec.).
- Example 3 (Beta diethylaminoethyl)-A -cycl0hexenylphenylacetonitrile was prepared from 41 g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 28.3 g. of diethylaminoethyl chloride and a suspension of 9.8 g. of sodium amide in 200 cc. of toluene by the method described in Example 1, part (b). The crude basic product, 52 g..was not purified but was used directly in the next reaction.
- Example 4 (a) (Beta-dimethylaminoezhyl)-A -cycl0pentenylphenylacet0nitrile.-To a stirred suspension of 18.7 g. of finely. divided sodium amide in 200 cc. of dry toluene was added 37.6 g. of the cyclopentylidenephenylacetonitrile of Example 2, part (a). After stirring for 30 minutes, 28.9 g. of dimethylaminoethyl chloride hydrochloride was added portionwise, and the reaction mixture was refluxed for five hours at 110 C. Alcohol was then added, followed by water to decompose excess sodium amide.
- Example5-' v v I (a) (Beta-dimethylarninoethyl) -A -cycl0hexenylphenylacetonitrile was prepared from 28.6v g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 20.9 g. of dimethylaminoethyl chloride hydrochloride and a suspension of 13.6 g. of sodium amide in 200 cc. of dry.toluene by the method described in Example 4, part (a). The 35.4 g. of basic product obtained was used directly in the next reaction. r
- Example 6 (a) A mixture of 22.2 g. of sodium dissolved in 580 cc. of absolute alcohol, 142.3 g. of m-methoxybenzyl cyanide and 97 g. of cyclohexanone was'caused to react in the manner described in Example 1, part (a), for the corresponding unsubstituted benzyl-cyanide. The product was distilled at reduced pressure giving 157 g., B. P. 152-159 C. (0.6 mm).
- P I (b) (Bera-piperidylethyl)-A -cyclohexenyl-m-methoxyphenylacetonitrile was prepared from 33.7 g.
- Example 7 V (a) (Gamma-piperzdylprapyl)-A cycl0hexenylphenyl acetonitrile was prepared from 296 g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 29.8 g. of N-piperidylpropyl chloride hydrochloride and a suspension of 14.0 g. of sodium amide in 200 cc. of toluene by the method described in Example 4, part (a). The 39.5 g. of crude basic product obtained was used directly in the next reaction.
- a cyclohexenylm meth'oxyphenylacetonitrilev was prepared from 33.7 g. of the cyclohexylideneor cyclohexenyl-m-methoxyphenylacetonitrile of Example 6, part (a), 21.7 g. of di- 7 methylaminoethyl .chloride hydrochloride and asuspension. of 14'. g. of; sodium. amide in 200 cc. of toluene by the method described [in Example 4-, part (a). The 32.9 g. of crude basic product thus obtained was used directly in the next reaction.
- Example 9 (a) (Beta pyrrolidylethyl) A cyclohexenylphenylaoetonitrile was prepared from 29.6 got the cyclohexylidenephenylacetonitrile of Example 1, part (a), 25.6 g. of N-pyrrolidylethyl chloride hydrochloride and a suspension of 14.0 g. of sodiumamide in 200 cc. of toluene by the, method described in Example. 4, part (a). The 38.7" g. of crude basic product thus: obtained was used directly in the next reaction.
- Example 10 (a) A. mixture of 20.2. g. of sodium' dissolved in 525 cc. of. absolute. alcohol, ,129 g. of p-methoxybenzyl cyanide and. 73.5 g. of cyclopentanone was caused to react in the: manner described in. Example 1, part (a). The distilled product solidified, M. P; 6466 C.
- Example 11 react in the manner described in Example 1, part (a).
- Example 12 (a) (Beta piperidylethyl) A cyclopentenyl (2- thienyl) acetonitrile was prepared from 24 g. of the cyclopentylideneor A -cyclopentenyl-(2-thienyl)-acetonitrile prepared in Example 11, part (a), 23.3 g. of N piperidylethyl chloride hydrochloride and a suspension of 12 g. of sodium amide in 200 cc. of dry toluene by the method described in Example 4, part (a). The crude base thus obtained was used directly in the next reaction.
- Example 13 (a) A cyclopentenylphenylacet0nitrile.-To a stirred suspension of finely divided sodium amide in 200 cc. of dry toluene was added 100 g. of benzyl cyanide, keeping'the temperature below 40 C. After stirring for onehalf hour, 87.4 g. of A -cyclopentenyl chloride was slowly added at a temperature below 30 C. The reaction mixture was stirred for sixteen hours, cooled, diluted with water andacidified with dilute hydrochloric acid. The product was extracted thoroughly with ether, and the ether layer was washed with water, sodium bicarbonate olution and again with water and dried over anhydrous sodium sulfate. After removal of the volatile solvent the residue was distilled twice at reduced pressure, giving 85.6 g'.-(54.5%) of A -cyclopentenylp'henylacetonitrile; B. P. l44151 C. (8 mm.).
- Example 14 (a) A -cyclhexenylphenylacetonitrile was prepared from 100 g. of benzyl cyanide, 137.1 g. of A -cyclohexenyl bromide and a suspension of 40 g. of sodium amide in 250 cc. of dry toluene by the same method used in Example 13, part (a) for the corresponding cyclopentenyl compound. The product was distilled at reduced pressure giving 88.2 g., B. P. 168-174 C.
- Example 15 (Beta piperidylethyl) A cyclopentenylphenylacetonitrile was prepared by a method similar to that described in Example 4, part (a). Its hydrochloride had the M. P. 229.5-231" C.
- a water-soluble salt of a compound of the formula wherein R is phenyl, Y is ethylene, N B is piperidino, and R is cyclopentenyl.
- a water-soluble salt of a compound of the formula wherein R is phenyl, Y is ethylene, N B is piperidino, and R is cyclohexenyl.
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Description
aile nm,
United States Patent 'ice ARYEDCYCLOALKENYL-TER'IIARY-AMINOALKYL ACETON'ES Sydney Archer and Arlo Wayne Ruddy, Albany, N. Y.,
assignors to Sterling Drug, Inc., Wilmington, Del., a corporation of Delaware No Drawing. Application August 5, 1952, Serial No. 306,486
9 Claims. or. 260-293) uable therapeutic agents and particularly useful'as anti- 1 spasmodics and antihistaminic agents, especially when employed in the form of water-soluble salts such as acid addition salts or quaternary ammonium salts.
These compounds have one of the following general formulas.
ti ycloalkylidene eyclyalkenyl These structures are isomeric, differing only in the position of the olefinic linkage: in Formula a the double bond is exocyclic, in Formula b endocyclic. The cycloalkylidene and cycloalkenyl radicals may contain five or six carbon atoms and R represents an aromatic group. The term aromatic embraces aryl groups such as phenyl, substituted phenyl, naphthyl, xenyl, etc. as Well as certain heterocyc'lic groups such as thienyl, pyridyl, furyl, etc. Y is an alkylene bridge of 2-3 carbon atoms and N=B is a tertiary-amino group. Specific examples of the group N=B include dimethylamino, ethylmethylamino, diethylamino, dipropylamino, dibutylamino, piperidyl, 2-methylpiperidyl, pyrrolidyl, Z-methylpyrrolidyl, morpholinyl, etc. These may be classed together as aliphatic tertiary-amino groups; the heterocyclic rings are distinctly non-aromatic in character and can be thought of as two alkyl groups joined together by a divalent bridge such as CI-L'-, O- or S.
Reactions expected to produce compounds of the formula I or II:
sometimes lead to the isolation of the compound corresponding to I, or may produce a compound with the Formula II. The following explanation will make this matter clear. These structures are isomeric; they difier in the position of the double bond, but are interchangeable by a simple shift of a hydrogen atom. In a reaction medium of the sort used in thesesnytheses in which a strong base is present, a tautomeric equilibrium is set up between these two forms. The relative amounts of the two forms present at equilibrium, depend upon the species involved, and the form actually isolated depends not only upon this ratio but upon the physical properties of the two forms. The more insoluble, more easily crystallizable form will be more readily isolated. This multiplicity of variables makes it difiicult to predict whether the final 2,762,812 Patented Sept. 11, 1956 product will have the structure I or II. Once obtained, the structure of thecompound can readily be proved by oxidation studies. Selective oxidation using ozone or potassium permanganate causes cleavage of the molecule at the double bond and the introduction of a carbonyl or carboxyl group at the points of cleavage. The Formula I when subjected to such an oxidation gives a basic ketone and a neutral moiety, either cyclopentanone or cyclohexanone, both easily identified. Formula II upon such oxidation gives an amino aldehyde or an amino acid and no neutral material. Moreover, we have found that in many cases, the ultra-violet absorption spectra will reveal the position of the double bond in these two alternative structures. Formula I has the double bond in conjugation with the aromatic nucleus and tends to show a maximum of absorption at 240-250 mg with the logarithm of the molar extinction coeflicient (log EM) approximately 4, similar to that shown by styrene and substituted styrenes. In Formula II the double bond is isolated and the value of log EM in the neighborhood of 240-250 m tends to be much lower.
These compounds are generally used in the form of water-soluble salts such as those produced by the addition of acids. The acids which may be used to prepare the salts are those which produce, when combined with the free bases, salts whose anions are relatively innocuous to the animal organism in therapeutic doses of the salts, so that the beneficial physiological properties inherent in the free bases are not vitiated by side-efiects ascribable to the anions. Appropriate acid addition salts are those derived from mineral acids such as hydrochloric acid, hydrobromic acid, hydriodic acid and sulfuric acid; and organic acids such as acetic acid, citric acid and tartaric aid. Our compounds may also be used in the form of ammonium salts derived from lower alkyl esters of strong inorganic acids, organic sulfonic acids and the like, such as methyl chloride, methyl bromide, methyl iodide, ethyl bromide, ethyl iodide, propyl bromide, propyl iodide, methyl sulfate, methyl benzenesulfonate, methyl p-toluenesulfonate, etc.
Our compounds show consistently high antispasmodic and moderate antihistaminic activity. They are effective both against barium chloride induced spasms (musculotropic), showing'from ten to seventy times the activity of papaverine; and against acetylcholine induced spasms (neurotropic), showing from one to eight percent of the activity of atropine. Although atropine possesses a considerably higher neurotropic activity than our compounds and other synthetic antispasmodics, it produces many undesirable physiological side-efli'ects. It is therefore highly desirable to vfind synthetic drugs which do not induce these characteristic side reactions in the organism.
Histamine has been demonstrated to play an important role in allergenic reactions, and it has been found that substances which are antagonistic to histamine often cause marked amelioration of symptoms. Our compounds have been found to be five to fifty times as efliective as papavcrime in counteracting the physiological eflFects of histamine.
Compounds of the Formulas I and II may be synthesized in the following manner. An aromatically monosubstituted acetonitrile is condensed with a cycloalkanone in the presence of a basic catalyst. The elements of water split out and the compound (III) is formed.
Specific examples of the formula RCHzCN which may be used are phenylacetonitrile, p-anisylacetonitrile, manisylacetonitrile, p-tolylacetonitrile, l-naphthalencacetonitrile, Z-naphthaleneacetonitrile, Z-thiopheneacetonitrile, 3-thiopheneacetonitrile, Z-furanacetonitrile, 3-furanacetonitrile, Z-pyridineacetonitrile and 4-pyridineacetonitrile.
The expected structure is that of Formula III(a). However, a tautomeric shift of a hydrogen atom leads to the formation of the structure III(b) to a greater or less extent.
The compound III is then alkylated with a tertiaryaminoalkyl halide in the presence of a strong basic catalyst such as sodium amide, giving a trisubstituted acetonitrile (IV). In the following equation X is a halogen Specific examples of the compound XY-N=B, where X is halogen (preferably chlorine, bromine or iodine) include beta-diethylaminoethyl halide, beta-dimethylaminoethyl halide, beta-(ethylmethylamino)-ethyl halide, beta-dipropylaminoethyl halide, beta-dibutylaminoethyl halide, 3-dimethylamino-l-halopropane, 3-diethylamino-l-halopropane, 1-dimethylamino-Z-halopropane, 1- diethylamino-Z-halopropane, 2-dimethylamino-1-halopropane. Z-diethylaminol-halopropane, beta-(N-piperidyl)- ethyl halide, 3-(N-piperidyl)-1-halopropane, l-(N-piper- 'idyl)-2-halopropane, 2-(N-piperidyl)-1-halopropane, beta- (N-pyrrolidyl)-ethyl halide, 3-(N-pyrrolidyl)-1-halopropane, *beta-N-(Z-methylpiperidyl)-ethyl halide, beta-N-(2- methylpyrrolidyl) -ethyl halide, beta-(N-rnorpholinyl) -eth yl halide, 3-(N-rnorpholinyl)-l-halopropane, etc.
In compound IV there is no alternative structure. The double bond must be within the alicyclic ring. The final step of the synthesis involves removal of the cyanide group and its replacement by hydrogen. This is accomplished by heating the nitrile with sodium amide in a suitable inert solvent such as toluene or xylene.
Again, with a hydrogen restored to the central carbon atom, a tautomeric shift is possible, resulting in the alternative structures, I and II. The structure which is formed to the greater extent or is more easily isolated in the form of an acid-addition salt, depends upon the individual species involved, since for each species the equilibrium ratio of the two forms will be different as Well as the solubility relationships of the salts.
Compounds in which the double bond is within the alicyclic ring but does not include the carbon atom which joins the ring with the remainder of the molecule can be synthesized by the methods just described wherein a cycloalkenyl halide is employed in place of a cycloalkanone. In this case the cycloalkenyl halide has the double bond in the beta-gamma or gamma-delta position with respect to the halogen atom. In these compounds the double bond is isolated and has little opportunity to rearrange, giving a final product whose complete structure is known without further investigation.
The following examples illustrate reactions carried out by us for the preparation of the compounds of our invention. The scope .of the invention, however, should not be strictly limited to the specific compounds shown herein.
Example 1 (a) Cyclohexylidenephenylacetonitrile.-In a 2-liter, 3-necked flask, equipped with a stirrer, thermometer and dropping funnel, was placed 600 cc. of absolute ethyl alcohol, and 23 g. of sodium was dissolved therein. Benzyl cyanide (117 cc.) was then added, and, after cooling the mixture to room temperature, g. of cyclohexanone was added gradually through the dropping funnel with stirring. The reaction mixture was refluxed for 45 minutes, cooled, diluted with water and acidified with dilute hydrochloric acid. The product was extracted thoroughly with ether, and the ether layer was washed with water, sodium bicarbonate solution and again with water and dried over anhydrous sodium sulfate. After removal of the volatile solvent the residue was distilled twice at reduced pressure giving 89.5 g. of cyclohexylidenephenylacetonitrile, B. P. l25-13l C. (0.7 rnrn.).
(b) (Beta piperidylethyl) A cyclohexenylphenylucet0nitrile.To a stirred suspension of 11.7 g. of finely divided sodium amide in 200 cc. of dry toluene contained in a S-necked flask equipped with a thermometer and dropping funnel, was added 49.3 g. of the product obtained in part (a). After warming the mixture to 70 C., 37 g. of N-piperidylethyl chloride in 50 cc. of dry toluene was added dropwise, and the reaction mixture was refluxed for sixteen hours. Alcohol was then added, followed by water in order to decompose excess sodium amide. This was extracted with ether and the ether extracts washed with dilute hydrochloric acid. The acid washings were made basic with dilute sodium hydroxide and the liberated organic base extracted with ether. The ether extracts were washed with water and dried over anhydrous sodium sulfate. The ether was removed by distillation, and the crude residue of (beta-piperidylethyl)- A -cyclohexenylphenylacetonitrile was converted to its hydrochloride by adding dilute hydrochloric acid in excess and stirring until crystalline. Filtration and drying gave 79.2 g. of crystalline hydrochloride, which upon recrystallization from dilute hydrochloric acid had the M. P. 206-208 C.
(c) 1 (N piperidyt) 3 phenyl 3 (A cyclohexcnyl)-pr0pane.-T0 a stirred suspension of 19.5 g. of finely divided sodium amide in 250 cc. of dry toluene was added 25.8 g. of (beta-piperidylethyl)-A -cyclohexenylphenylacetonitrile (obtained from the hydrochloride of part (b) by the addition of excess sodium hydroxide, extraction with ether, careful drying and isolation of the free base). The mixture was refluxed for twelve hours, cooled and mixed with alcohol and water to decompose excess sodium amide. This was extracted with ether, and the ether extracts washed with dilute hydrochloric acid. The acid washings were made basic with dilute sodium hydroxide and the liberated organic base extracted with ether. The ether extracts were washed with water and dried over anhydrous sodium sulfate. The ether was removed and the residue distilled at reduced pressure, giving 13.5 g. of amine, B. P. l69l72 C. (1.5 rnm.). Upon dissolving this in dilute hydrochloric acid and cooling, the hydrochloride of the amine precipitated. This was filtered and recrystallized twice from dilute hydrochloric acid giving 10 g. of the hydrochloride of l-(N- piperidyl)-3-phenyl-3-(h -cyclohexenyl)-propane, M. P. 244-246" C.
Example 2 addition of petroleum ether (B. P. 60-70 C.) caused crystallization of phenyl acetamide which was removed by filtration. Redistillation of the filtrate gave 47 g. of cyclopentylidenephenylacetonitrile, B. P. 155-169 'C. (0.6 mm.).
(b.) (Beta-piperidylethyl)-A -cyl0pentenylphenylacetonitrile was prepared from 47 g. of the cyclopentlyidenephenylacetonitrile of part (a), 38 g. of N-piperidyletbyl chloride and a suspension of 11.7 g. of sodium amide in toluene by the method described in Example 1, part (b). The crude amine, 59.8 g., was not converted to the hydrochloride but was used directly in the next reaction.
(0) 1-(N-piperidly)-3-phenyl 3 (A cyclopentenyl)- propane was prepared from 59.8 g. of crude (beta-piperidylethyl)-A -cyclopentenylphenylacetonitrile and a suspension of 31.2 g. ofsodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The free base distilled at 132140 C. (0.4 mm.). The hydrochloride was prepared by dissolving the free amine in dry ether and adding an excess of alcoholic hydrogen chloride- The crude solid which precipitated was filtered, recrystallized'once from isopropyl alcohol and twice from an absolute alcohol-dry ether mixture, giving 3.7 g. of the hydrochloride of l-(N-piperidyl)-3-phenyl-3-(A -cyclopentenyl)-propane, M. P. 227 C. (dec.).
- Example 3 (a) (Beta diethylaminoethyl)-A -cycl0hexenylphenylacetonitrile was prepared from 41 g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 28.3 g. of diethylaminoethyl chloride and a suspension of 9.8 g. of sodium amide in 200 cc. of toluene by the method described in Example 1, part (b). The crude basic product, 52 g..was not purified but was used directly in the next reaction.
(b) 1-diethylamin0-3-phenyl-3-(A -cyclohexenyl) -pr0- pane was prepared from 52 g. of crude (beta-diethylaminoethyD-A -cyclohexenylphenylacetonitrile and a suspension of 27.3 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The free base distilled at 128133 (0.7 mm.) and amounted to 25.2 g. The hydrochloride was prepared by dissolving the free amine in dry ether and adding an excess of alcoholic hydrogen chloride. The crude solid which precipitated was filtered, giving 21 g., M. P. 114-117 C. When recrystallized twice from a mixture of absolute alcohol and absolute ether'it melted at 127-129 C.
Example 4 (a) (Beta-dimethylaminoezhyl)-A -cycl0pentenylphenylacet0nitrile.-To a stirred suspension of 18.7 g. of finely. divided sodium amide in 200 cc. of dry toluene was added 37.6 g. of the cyclopentylidenephenylacetonitrile of Example 2, part (a). After stirring for 30 minutes, 28.9 g. of dimethylaminoethyl chloride hydrochloride was added portionwise, and the reaction mixture was refluxed for five hours at 110 C. Alcohol was then added, followed by water to decompose excess sodium amide. This was extracted with ether and the ether extracts washed with dilute hydrochloric acid. The acid washings were made basic with dilute sodium hydroxide and the liberated organic base extracted with ether. These ether extracts were washed with water and dried over anhydrous sodium sulfate. The ether was removed by distillation leaving 38 g. of crude (beta-dimethylaminoethyl)-A -cyclopentenylphenylacetonitrile, which was used directly in the next reaction.
(b) 1 dimethylamin0-3-phenyl-3-cycl0pentylidenepr0 pane was prepared from 38 g. of crude (beta-dimethylaminoethyl)-A -cyclopentenylphenylacetonitrile and a suspension of 23.4 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The free base, 21.4 g., distilled at l119 C. (0.5 mm.). A refractionation gave 18.3 g., B. P. 109-112 C. (0.5 mm.).' The hydrochloride was prepared by the dry etheralcoholic hydrogen chloride method. When recrystallized three times from an alcohol-ether mixture, the hydrochloride of 1-dimethylamino-3-phenyl-3 cyclopentylidenepropane was'obtained in pure form," M. P. 202- 20 4 C. (dec 'I v I A sample of the hydrochloride was treated with an excess of aqueous potassium permanganate solution, and the mixture was steam distilled- From the distillate was isolated considerable amounts of cyclopentanone, identified asthe dibenzal-derivative, therebyproving the exoc'yclic position of.-the double bond in theamine hydro-. chloride.
: Example5-' v v I (a) (Beta-dimethylarninoethyl) -A -cycl0hexenylphenylacetonitrile was prepared from 28.6v g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 20.9 g. of dimethylaminoethyl chloride hydrochloride and a suspension of 13.6 g. of sodium amide in 200 cc. of dry.toluene by the method described in Example 4, part (a). The 35.4 g. of basic product obtained was used directly in the next reaction. r
(b) 1-dimethylamino-3-phenyl 3 A -cyclohexenyhpropane was prepared from 35.4 g. of crude (beta-dimethylaminoethyl)-A -cyclohexenylphenylacetonitrile and a suspension of 20.5 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The basic product was distilled twice at reduced pressure giving 15.4 g., B. P. -137 (1.0 mm). This was converted to its hydrochloride by the ether-alcoholic hydrogen chloride method, giving, after two recrystallizations from ethyl acetate, 10.2 g., M. P. 141.5144 C.
, Example 6 (a) A mixture of 22.2 g. of sodium dissolved in 580 cc. of absolute alcohol, 142.3 g. of m-methoxybenzyl cyanide and 97 g. of cyclohexanone was'caused to react in the manner described in Example 1, part (a), for the corresponding unsubstituted benzyl-cyanide. The product was distilled at reduced pressure giving 157 g., B. P. 152-159 C. (0.6 mm). P I (b) (Bera-piperidylethyl)-A -cyclohexenyl-m-methoxyphenylacetonitrile was prepared from 33.7 g. of thecyclohexylideneor cyclohexenyl-m-methoxyphenylacetonitrile of part (a), 22.2 g. of N-piperidylethyl chloride and a suspension of 7 g. of sodium amide in 200 cc. of toluene byv the method described in Example 1, part (b). The crude basic product, 41.8 g., was used directly in the next reaction.
(c) I-(N-piperidyl) -3-(m-methoxyphenyl-3-(A -cycl0- hexenyl)-propane was prepared from 41.8 g. of crude (beta piperidylethyl) -A -cyclohexenyl-m-methoxyphenylacetonitrile and a suspension of 19.3 g. of sodium amide in 200 cc. of dry toluene by the method described in Example 1, part (c). The free base was distilled at reduced pressure, B. P. 174-190 C. (0.7 mm.). The hydrochloride of the base was prepared by the etheralcoholic hydrogen chloride method. After two recrystallizations from an ether-alcohol mixture and one from a benzene-petroleum ether mixture, 38 g. of the hydrochloride, M. P. 192.5193{ C. was obtained.
Example 7 V (a) (Gamma-piperzdylprapyl)-A cycl0hexenylphenyl acetonitrile was prepared from 296 g. of the cyclohexylidenephenylacetonitrile of Example 1, part (a), 29.8 g. of N-piperidylpropyl chloride hydrochloride and a suspension of 14.0 g. of sodium amide in 200 cc. of toluene by the method described in Example 4, part (a). The 39.5 g. of crude basic product obtained was used directly in the next reaction.
(b) I-(N-piperidyl)-4-phenyl-4- (A -cycl0hexenyl)-butane was prepared from 39.5 g. of crude (gamma-piperidylpropyl)-A -cyclohexenylphenylacetonitrile and a suspension of 20 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The crude basic product was distilled at reduced pressure giving. 16.1 g., B. P.. l78-1'86 C. (1 mm.). Its hydrochloride was. prepared by the: ether-alcoholic hydrogen chloride method, giving. 16.7 g. of crude material, M. P. 142173 C. Three recrystallizations from ethylacetate gave a pure sample of the hydrochloride, P. 162- Example 8 (a): (Beta dimethylaminoethyl'). A cyclohexenylm meth'oxyphenylacetonitrilev was prepared from 33.7 g. of the cyclohexylideneor cyclohexenyl-m-methoxyphenylacetonitrile of Example 6, part (a), 21.7 g. of di- 7 methylaminoethyl .chloride hydrochloride and asuspension. of 14'. g. of; sodium. amide in 200 cc. of toluene by the method described [in Example 4-, part (a). The 32.9 g. of crude basic product thus obtained was used directly in the next reaction.
(b) 1 dimethylamino 3 (m methoxyphenyl) 3 (A cyclohexenyl) propane was prepared from 32.9 g. of crude (beta-dimethylaminoethyl)-A -cyclohexenylm-methoxyphenylacetonitrile and a suspension of 17.5 g. ofsodium. amide in 200 cc. of dry toluene by the method described in. Example 1,.part (c). The crude basic product was distilled at reduced pressure, B. P. 133-153" C. (0.8. mm.)- Its hydrochloride was. prepared by the etheralcoholic hydrogen. chloride method. After recrystallatiorrfr'om a benzene-petroleum ether mixture and from ethyl acetate, a pure sample of the hydrochloride was obtained, M. P. 126128 C.
Example 9 (a) (Beta pyrrolidylethyl) A cyclohexenylphenylaoetonitrile was prepared from 29.6 got the cyclohexylidenephenylacetonitrile of Example 1, part (a), 25.6 g. of N-pyrrolidylethyl chloride hydrochloride and a suspension of 14.0 g. of sodiumamide in 200 cc. of toluene by the, method described in Example. 4, part (a). The 38.7" g. of crude basic product thus: obtained was used directly in the next reaction.
(b) A mixture of 38.7 g. of crude (beta-pyrrolidylethyl)-Al-cyclohexenylphenylacetonitrile and a. suspensionof 20.5 g. of sodium amide in-250 cc. of dry toluene was caused to react; in themanner described'in Example 1, part; The. crude basic product was distilled at reduced pressure, giving 18.4 g., B. P. l49'-153 C. (0.7 mm.). Its hydroehloride was prepared by the: etheralcoholic hydrogen chloride method, giving 19.6 g. of crude .material, MVP. 173l81 C. Two-recrystallizations'. from. an alcohol-ether mixture: gave g;, M; P. 189--19-l- C. of. what is the hydrochloride ofeither 1- (N-pyrrolidyl)-3-phenyl?3-cyclohexylidenepropane or 1- (N-pyrrolidyl) -3-phenyl-3- (A -cyclohexenyl) -prop ane.
Example 10 (a) A. mixture of 20.2. g. of sodium' dissolved in 525 cc. of. absolute. alcohol, ,129 g. of p-methoxybenzyl cyanide and. 73.5 g. of cyclopentanone was caused to react in the: manner described in. Example 1, part (a). The distilled product solidified, M. P; 6466 C.
(b) (Beta-dimethylaminoethyl) A cyclopentenylp methoxyphenylacetonitrile was prepared from 11.2 g. ofthe cyclopentylideneor cyclopentenyl p-methoxyphenylacetonitrile of part (a), 7.6 g. of dimethylaminoethyl chloride hydrochloride and a suspension of 5 g. of. sodium amide. in. 150 cc. of' toluene by the. method described in Example 4; part (a). The crude basic prodnot; thus obtained was. used directly in the next reaction.
(c) 1 dimethylamino 3 (p methoxyphenyl) 3 cyclopentylidenepropane was prepared from the total crude (beta-dimethylaminoethyl) A cyclopentenyl pmethoxyphenylacetonitrile of part (1)) and a: suspension of 101gof sodium amidein 150 cc. of dry toluene byv the method' described inExample 1, part (c). The. crude basic product was converted directly to its.hydrochloride by the ether-alcoholic hydrogen chloride. method. Two
recrystallizationsof the crude material from ethyl acetate gave a pure sample of the hydrochloride, M. P. 185.5- 186.5 C.
Example 11 react in the manner described in Example 1, part (a).
Distillation of the product at reduced pressure gave 49 g., B. P. 143-150 C. This oil crystallized upon standing and when recrystallized from petroleum ether (B. P. 60- 70" C.) had the M. P. 4648 C.
, (b) (Beta dimethylaminoethyl) A cyclopentenyl- (2 thienyl) acetonitrile was prepared from 24 g. of the cyclopentyliden'eor A -cyclopentenyl-(2-thieny1) acetonitrile prepared in part (a), 18.2 g. of dimethylaminoethyl chloride hydrochloride and a suspension of 12 g. of sodium amide in 200 cc. of dry toluene by the method described in Example 4, part (a). The crude base thus obtained was used directly in the next reaction.
(0) A solution of the crude (beta-dimethylaminoethyl)-A -cyclopentenyl-(Z-thienyl)-acetonitrile from part (b) in a suspension of 20 g. of sodium amide in 200 cc; of dry toluene was caused to react in the manner described in Example 1, part (c). The crude base was distilled at reduced pressure, B. P. -150 C. (1 mm.). This was converted to its hydrochloride by the etheralcoholic hydrogen chloride method. The crude material, 11.5 g., was recrystallized from an alcohol-ether mixture and leached with ethyl acetate to remove unchanged ni-. trile. A pure sample of the hydrochloride of whatis either 1-dimethylamino-3-(Z-thienyl)-3-cyclopentylidenepropane or 1-dimethylamino-3-(Z-thienyl)-3-(A -cyclopentenyl)-propane had the M. P. 200.5203.5 C.
Example 12 (a) (Beta piperidylethyl) A cyclopentenyl (2- thienyl) acetonitrile was prepared from 24 g. of the cyclopentylideneor A -cyclopentenyl-(2-thienyl)-acetonitrile prepared in Example 11, part (a), 23.3 g. of N piperidylethyl chloride hydrochloride and a suspension of 12 g. of sodium amide in 200 cc. of dry toluene by the method described in Example 4, part (a). The crude base thus obtained was used directly in the next reaction.
(b) A solution of the crude (beta-piperidylethyD-A cyclopentenyl-(Z-thienyl)-acetonitrile from part (a) in a suspension of 20 g. of sodium amide in 200 cc. of dry toluene was caused to react in the manner described in Example 1, part (c). The free base was distilled at reduced pressure, B. P. 165 C. (12 mm.). This was converted to its hydrochloride by the ether-alcoholic hydrogen chloride method. The crude material, 12 g., was recrystallized three times from ethyl acetate, giving a pure sample of what is either 1-(N-piperidy1)-3 (2- thienyl)-3-cyclopentylidenepropane hydrochloride or 1- (N-piperidyl) -3-(2-thienyl)-3 (A cyclopentenyl) propane hydrochloride, and having the M. P. 166168.5 C.
Example 13 (a) A cyclopentenylphenylacet0nitrile.-To a stirred suspension of finely divided sodium amide in 200 cc. of dry toluene was added 100 g. of benzyl cyanide, keeping'the temperature below 40 C. After stirring for onehalf hour, 87.4 g. of A -cyclopentenyl chloride was slowly added at a temperature below 30 C. The reaction mixture was stirred for sixteen hours, cooled, diluted with water andacidified with dilute hydrochloric acid. The product was extracted thoroughly with ether, and the ether layer was washed with water, sodium bicarbonate olution and again with water and dried over anhydrous sodium sulfate. After removal of the volatile solvent the residue was distilled twice at reduced pressure, giving 85.6 g'.-(54.5%) of A -cyclopentenylp'henylacetonitrile; B. P. l44151 C. (8 mm.).
(b) (Beta dimethylaminoethyl) A cyclopentenylphenylacetonitrile was prepared from 29 g. of A cyclopentenylphenylacetonitrile,. 22.7 g. of dimethylaminoethyl chloride hydrochloride and a suspension of 15 g. of sodium amide in250'cc. 'of dry toluene by the method described in Example 4, part (a). The crude base thus obtained was used directly in the next reaction. A sample was converted to its hydrochloride which when purified had the M. P. 214.5216.5 C.
(c) 1 dimethylamino 3 phenyl 3 (A cyclopentenyl) propane was prepared from the total crude (betadimethylaminoethyl) A cyclopentenylphenylacetonitrile of part (b) and a suspension of 25 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 1, part (c). The basic product was distilled at reduced pressure giving 23.5 g. (65%), B. P. 116-117 C. (1 mm). Part of this, 18.5 g., was converted to its hydrochloride by the ether-alcoholic hydrogen chloride method, giving 14.6 g. of crude crystalline product, M. P. 114123 C. Two recrystallizations of this from ethyl acetate gave a pure sample of the hydrochloride, M. P. 129-132 C.
(d) Methiodide of .I-dimethylamino-3-phenyl-3-(A -cyclopentenyl)pr opane.-A solution of 5 g. of l-dimethylamino-3-phenyl-3-(A -cyclopenteny1)propane and 5 cc. of methyl iodide in 25 cc. of acetone was allowed to stand overnight. Upon adding ether to the filtrate, the methiodide precipitated and was filtered, giving 8 g., M. P. 122- 128 C. After one recrystallization from an acetone-ether mixture and two recrystallizations from water, 2 g. of pure methiodide, M. P. 171173.5 C. was obtained.
Example 14 (a) A -cyclhexenylphenylacetonitrile was prepared from 100 g. of benzyl cyanide, 137.1 g. of A -cyclohexenyl bromide and a suspension of 40 g. of sodium amide in 250 cc. of dry toluene by the same method used in Example 13, part (a) for the corresponding cyclopentenyl compound. The product was distilled at reduced pressure giving 88.2 g., B. P. 168-174 C.
(b) (Beta piperidylethyl) A cyclohexenylphenylacetonitrile was prepared from 44.1 g. of A -cyc1ohexeny1- phenylacetonitrile, 41 g. of N-piperidylethyl chloride hydrochloride and a suspension of 21 g. of sodium amide in 250 cc. of dry toluene by the method described in Example 4, part (a). The crude basic product was used directly in the next reaction. The hydrochloride of (betapiperidylethyl)A -cyclohexenylphenylacetonitrile had the M. P. 216-218 C. (uncorr.). The methiodide had the M. P. 158160 C.
(c) 1 (N piperia'yl) 3 phenyl 3 (A cyclohexenyl)-pr0pane was prepared from the crude (beta-piperidylethyl)M-cyclohexeuylphenylacetonitrile of part (b) and a suspension of 34 g. of sodium amide in 300 cc. of toluene by the method of Example 1, part (c). The basic product was distilled at reduced pressure to give 18.8 g., B. P. 163-170 C. (1.1 mm). This was converted to its hydrochloride by the ether-alcoholic hydrogen chloride method, giving 15.2 g. of crude crystalline product, M. P. 114-123 C. One recrystallization from ethyl acetate gave a pure sample of the hydrochloride of l-(N- piperidyl)3-phenyl-3-(A -cyclohexenyl)propane, M. P. l82-184 C. (uncorr.).
Example 15 (Beta piperidylethyl) A cyclopentenylphenylacetonitrile was prepared by a method similar to that described in Example 4, part (a). Its hydrochloride had the M. P. 229.5-231" C.
This application is a division of our copending application Serial No. 52,432, filed October 1, 1948, now U. S. Patent 2,647,122.
1. A c'tmipt'n'lnd"selectedfrom the'group consisting of basic nitriles of the formula YN=B wherein R is an aromatic group selected from the group consisting of the benzene, naphthalene, biphenyl, thiophene, pyridine and furan series, Y is an alkylene bridge of from 2 to 3 carbon atoms, N=B is a member of the group consisting of di-lower-alkylamino, piperidino, pyrrolidino, rnorpholino, and lower-alkylated piperidino, pyrrolidino and morpholino radicals, and R is a cycloalkenyl group selected from the group consisting of cyclopentenyl and cyclohexenyl; and water-soluble salts thereof.
2. A water-soluble salt of a compound of the formula ON R J Y N=B wherein R is phenyl, Y is ethylene, N=B is di-loweralkylamino, and R is cyclopentenyl.
3. A water-soluble salt of a compound of the formula ON R-b'-Y-N=B wherein R is phenyl, Y is ethylene, N=B is di-loweralkylamino, and R is cyclohexenyl.
4. A water-soluble salt of a compound of the formula wherein R is phenyl, Y is ethylene, N=B is piperidino, and R is cyclopentenyl.
5. A water-soluble salt of a compound of the formula wherein R is phenyl, Y is ethylene, N=B is piperidino, and R is cyclohexenyl.
6. A water-soluble salt of (beta-piperidylethyl)-A -cyclohexenylphenylacetonitrile having the formula 7. A water-soluble salt of (beta-dimethylaminoethyl)- A -cyclopentenylphenylacetonitrile having the formula 8. A water-soluble salt of (beta-piperidylethyl)-A -cyclohexenylphenylacetonitrile having the formula 11 12 9. A water-soluble salt of (beta-piperidylethyl)-4 -cy- 7 References Cited in the file of this patent qlopentenylphepylacetqnitrile having the formula v UNITED STATES PATENTS E fi fi 2,446,804 Bergel et a1; Aug. 10, 1948 mm-o-omonm /CH1 5 2,542,466 Blicke Feb. 20, 1951 H CHaCH:
Claims (1)
1. A COMPOUND SELECTED FROM THE GROUP CONSISTING OF BASIC NITRILES OF THE FORMULA
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3125573A (en) * | 1964-03-17 | chzchz | ||
US4065501A (en) * | 1974-03-22 | 1977-12-27 | Asta-Werke Aktiengesellschaft | Basic enol ether and acid addition salts thereof |
US4124716A (en) * | 1974-03-22 | 1978-11-07 | Asta-Werke Aktiengesellschaft | Process for the treatment of spasmodic conditions in humans |
US20080200554A1 (en) * | 2005-06-16 | 2008-08-21 | Givaudan Sa | Cycloaklyldiene-(Ortho Substituted Phenyl)-Acetonitriles and Their Use as Odorants |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2446804A (en) * | 1943-03-09 | 1948-08-10 | Hoffmann La Roche | 3-aryl-3-carbalkoxy piperidines and pyrrolidines and synthesis thereof |
US2542466A (en) * | 1947-08-23 | 1951-02-20 | Univ Michigan | Cyclohexyl-phenyl-aminoalkylketones and their production |
-
1952
- 1952-08-05 US US306486A patent/US2762812A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2446804A (en) * | 1943-03-09 | 1948-08-10 | Hoffmann La Roche | 3-aryl-3-carbalkoxy piperidines and pyrrolidines and synthesis thereof |
US2542466A (en) * | 1947-08-23 | 1951-02-20 | Univ Michigan | Cyclohexyl-phenyl-aminoalkylketones and their production |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3125573A (en) * | 1964-03-17 | chzchz | ||
US4065501A (en) * | 1974-03-22 | 1977-12-27 | Asta-Werke Aktiengesellschaft | Basic enol ether and acid addition salts thereof |
US4124716A (en) * | 1974-03-22 | 1978-11-07 | Asta-Werke Aktiengesellschaft | Process for the treatment of spasmodic conditions in humans |
US20080200554A1 (en) * | 2005-06-16 | 2008-08-21 | Givaudan Sa | Cycloaklyldiene-(Ortho Substituted Phenyl)-Acetonitriles and Their Use as Odorants |
US7655701B2 (en) | 2005-06-16 | 2010-02-02 | Givaudan Sa | Cycloalkylidene-(ortho substituted phenyl)-acetonitriles and their use as odorants |
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